Effect of the alkylidene spacer and the p-tert-butylthiacalix[4]arene macrocyclic platform on the reactivity of the hydroxyl groups in the acylation reaction
- Авторлар: Padnya P.1, Bayarashov Е.1, Potrekeeva О.1, Stoikov I.1
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Мекемелер:
- Butlerov Institute of Chemistry
- Шығарылым: Том 87, № 9 (2017)
- Беттер: 2111-2114
- Бөлім: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/221305
- DOI: https://doi.org/10.1134/S107036321709033X
- ID: 221305
Дәйексөз келтіру
Аннотация
A series of cone and 1,3-alternate p-tert-butylthiacalix[4]arenes tetrasubstituted at the lower rim simultaneously by the amide, ester, and carboxyl functions were synthesized. The reactivity of the synthesized compounds depends on the length of the alkylidene spacer. The N-(hydroxyethyl)amide derivatives do not react with succinic anhydride, whereas the N-(3-hydroxypropyl)amide derivatives react to form acylation products.
Негізгі сөздер
Авторлар туралы
P. Padnya
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
Ресей, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
Е. Bayarashov
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
Ресей, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
О. Potrekeeva
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
Ресей, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
I. Stoikov
Butlerov Institute of Chemistry
Хат алмасуға жауапты Автор.
Email: ivan.stoikov@mail.ru
Ресей, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008